Human Genome Epidemiology Literature Finder
Records 1 - 5 (of 5 Records) |
Query Trace: Abnormalities and TSC1[original query] |
---|
Clinical symptoms of tuberous sclerosis complex in patients with an identical TSC2 mutation. Medical science monitor : international medical journal of experimental and clinical research 2005 May 11 (5): CR230-234. Rok Paulina, Kasprzyk-Obara Jolanta, Doma?ska-Pakie?a Dorota, Jó?wiak Sergiu |
Genotype and brain pathology phenotype in children with tuberous sclerosis complex. European journal of human genetics : EJHG 2016 Jul . Overwater Iris E, Swenker Rob, van der Ende Emma L, Hanemaayer Kimberley Bm, Hoogeveen-Westerveld Marianne, van Eeghen Agnies M, Lequin Maarten H, van den Ouweland Ans Mw, Moll Henriëtte A, Nellist Mark, de Wit Marie-Claire |
Electro-clinical and neurodevelopmental outcome in six children with early diagnosis of tuberous sclerosis complex and role of the genetic background. Italian journal of pediatrics 2020 3 46 (1): 36. Savini M N, Mingarelli A, Peron A, La Briola F, Cervi F, Alfano R M, Canevini M P, Vignoli |
The association of neurodevelopmental abnormalities, congenital heart and renal defects in a tuberous sclerosis complex patient cohort. BMC medicine 2022 4 20 (1): 123. Robinson Jessica, Uzun Orhan, Loh Ne Ron, Harris Isabelle Rose, Woolley Thomas E, Harwood Adrian J, Gardner Jennifer Frances, Syed Yasir Ahm |
Genotype and Phenotype Landscape of 283 Japanese Patients with Tuberous Sclerosis Complex. International journal of molecular sciences 2022 10 23 (19): . Togi Sumihito, Ura Hiroki, Hatanaka Hisayo, Niida |
- Page last reviewed:Feb 1, 2024
- Page last updated:Apr 22, 2024
- Content source: